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POLIO MYELITIS
Saranya.v
18UT16
Pharmaceutical marketing
POLIOMYELITIS
INTRODUCTIION
• Poliomyelitis is a viral infection.
• The words polio means “grey” and myelin means “marrow indicating the spinal
cord” are derived from the Greek.
• Poliomyelitis literally meaning “ grey spinal cord inflammation”.
• A viral disease which may affect the spinal cord causing muscle weakness and
paralysis.
• Virus localized in the anterior horn cells of the spinal cord and certain brain steam
motor nuclei.
• 3 types : Spinal, Bulbar, Bulbo – spinal.
• Disease is more common in the summer (or) rainy season .
• The virus is
transmitted by
person to
person spread
mainly through
the fecal- oral
route or less
frequently by a
common vehicle
PATHOGENESIS
• The mouth is the portal of entry of the virus and primary multiplication of the virus
occurs at the site of implantation in pharynx and gastrointestinal track .
• The virus is usually present in the throat and in the stools before the onset of illness.
• One weeks after onset there is little virus in the throat but virus continues to be
excreted in the stools for several weeks .
• The virus invades local lymphoid tissue enters the blood streamand then may infect
cells of the central nervous system.
• Replication of polio virus in motor neurons of anterior horn and brain stem results in
cells destruction and causes the typical manifestation of poliomyelitis .
LABORATORY DIAGNOSIS
• Samples to be collected blood, CFS, throat swab, feces.
• Transport immediately to lab in viral transport media (Hanks Balanced Salt Solution)
• Storage 4 Degree C (days) -20degree C (months to year)
• There are tests available
• Viral Isolation
• Serologic testing
• Cerebrospinal fluid (CSF) analysis
Viral isolation :
The likelihood of polio virus isolation is highest from stool specimens
Intermediate from pharyngeal swahs &very low from blood or spinal
fluid.
Serologic testing :
Testin A four – fold title rise between the acuts & convalescent specimens
suggests polio virus infection.
Cerebral fluid (CSF) analysis :
The cerebrospinal fluid usually contains an increased number of leukocyte
from 10 to 200 cells/ mm3 and a mildly elevated protein from 40 to 50 mg/100 ml .
EPIDEMIOLOGY
• Agent : Polio virus
• Type : three types ( type 1,2,3)
• Reservoir : man
• Infectious materials : faeces,oro – pharynged secretions.
• Incubation period : 7 to 14 days
• Period of communicability : 7 to 10 days
• Host age : 6 months to 3 years.
• Environment : rainy season ( june to september )
• Mode of transmission : faeco – oral route, droplet infection
PREVENTION
• General prevention :
Health promotion through environment sanitation .
Health education ( mode of spread, protective value of vaccination)
• Specific protection :
Passive immunization by human immunoglobulin
• Dose : (0.25-0.3 ml/ kg of body weight)
• Schedules : given either or before or very shortly after exposure to infection (not practical
• Active immunization :
Salk vaccine (intra muscular trivalent killed vacc)
Sabin vaccine (oral polio trivalent live attenuated va.)
CONTROL
• Sabin’s live attenuated vaccine.
• Grown in monkey kidney cells.
• Human diploid cells preserved at 4 degree C
• Multiple doses are given as oral drops .
• At present only vaccine given in our national programme of iimmunization .
• Boosts immunity with production IgG,IgM.
• And also IgA participated in prevention .
Poliomyelitis
Poliomyelitis
Poliomyelitis

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Poliomyelitis

  • 3. INTRODUCTIION • Poliomyelitis is a viral infection. • The words polio means “grey” and myelin means “marrow indicating the spinal cord” are derived from the Greek. • Poliomyelitis literally meaning “ grey spinal cord inflammation”. • A viral disease which may affect the spinal cord causing muscle weakness and paralysis. • Virus localized in the anterior horn cells of the spinal cord and certain brain steam motor nuclei. • 3 types : Spinal, Bulbar, Bulbo – spinal. • Disease is more common in the summer (or) rainy season .
  • 4. • The virus is transmitted by person to person spread mainly through the fecal- oral route or less frequently by a common vehicle
  • 5. PATHOGENESIS • The mouth is the portal of entry of the virus and primary multiplication of the virus occurs at the site of implantation in pharynx and gastrointestinal track . • The virus is usually present in the throat and in the stools before the onset of illness. • One weeks after onset there is little virus in the throat but virus continues to be excreted in the stools for several weeks . • The virus invades local lymphoid tissue enters the blood streamand then may infect cells of the central nervous system. • Replication of polio virus in motor neurons of anterior horn and brain stem results in cells destruction and causes the typical manifestation of poliomyelitis .
  • 6.
  • 7. LABORATORY DIAGNOSIS • Samples to be collected blood, CFS, throat swab, feces. • Transport immediately to lab in viral transport media (Hanks Balanced Salt Solution) • Storage 4 Degree C (days) -20degree C (months to year) • There are tests available • Viral Isolation • Serologic testing • Cerebrospinal fluid (CSF) analysis
  • 8. Viral isolation : The likelihood of polio virus isolation is highest from stool specimens Intermediate from pharyngeal swahs &very low from blood or spinal fluid. Serologic testing : Testin A four – fold title rise between the acuts & convalescent specimens suggests polio virus infection. Cerebral fluid (CSF) analysis : The cerebrospinal fluid usually contains an increased number of leukocyte from 10 to 200 cells/ mm3 and a mildly elevated protein from 40 to 50 mg/100 ml .
  • 9. EPIDEMIOLOGY • Agent : Polio virus • Type : three types ( type 1,2,3) • Reservoir : man • Infectious materials : faeces,oro – pharynged secretions. • Incubation period : 7 to 14 days • Period of communicability : 7 to 10 days • Host age : 6 months to 3 years. • Environment : rainy season ( june to september ) • Mode of transmission : faeco – oral route, droplet infection
  • 10. PREVENTION • General prevention : Health promotion through environment sanitation . Health education ( mode of spread, protective value of vaccination) • Specific protection : Passive immunization by human immunoglobulin • Dose : (0.25-0.3 ml/ kg of body weight) • Schedules : given either or before or very shortly after exposure to infection (not practical • Active immunization : Salk vaccine (intra muscular trivalent killed vacc) Sabin vaccine (oral polio trivalent live attenuated va.)
  • 11. CONTROL • Sabin’s live attenuated vaccine. • Grown in monkey kidney cells. • Human diploid cells preserved at 4 degree C • Multiple doses are given as oral drops . • At present only vaccine given in our national programme of iimmunization . • Boosts immunity with production IgG,IgM. • And also IgA participated in prevention .